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| White matter disorders and cerebral calcification - narrow panel v1.208 | AP1S2 | Arina Puzriakova Publications for gene: AP1S2 were set to 17617514; 1842820 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| White matter disorders and cerebral calcification - narrow panel v1.207 | AP1S2 | Arina Puzriakova Phenotypes for gene: AP1S2 were changed from Calcifications in basal ganglia; Mental retardation, X-linked syndromic 5, 304340 to Pettigrew syndrome, OMIM:304340; Calcifications in basal ganglia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| White matter disorders and cerebral calcification - narrow panel v0.17 | AP1S2 | Louise Daugherty Phenotypes for gene: AP1S2 were changed from Calcifications in basal ganglia to Calcifications in basal ganglia; Mental retardation, X-linked syndromic 5, 304340 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| White matter disorders and cerebral calcification - narrow panel v0.11 | AP1S2 |
Ellen McDonagh gene: AP1S2 was added gene: AP1S2 was added to White matter disorders and cerebral calcification - narrow panel. Sources: Expert Review Green Mode of inheritance for gene: AP1S2 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) Publications for gene: AP1S2 were set to 17617514; 1842820 Phenotypes for gene: AP1S2 were set to Calcifications in basal ganglia |
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